Henrique Andrade Rodrigues da Fonseca
Federal University of São Paulo
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Diabetes and Vascular Disease Research | 2013
Maria Cristina de Oliveira Izar; Henrique Andrade Rodrigues da Fonseca; Luiz F Pinheiro; Carlos Manoel de Castro Monteiro; Rui Póvoa; Andrea Moreira Monteiro; Antônio Martins Figueiredo-Neto; Magnus Gidlund; Francisco Antonio Helfenstein Fonseca
Metabolic syndrome (MetS) is an inflammatory state associated with high coronary disease risk. Inflammation and adaptive immunity modulate atherosclerosis and plaque instability. We examined early changes in anti-oxidized low-density lipoprotein (LDL) (anti-oxLDL) autoantibodies (Abs) in patients with MetS after an acute coronary syndrome (ACS). Patients of both genders (n=116) with MetS were prospectively included after an acute myocardial infarction (MI) or hospitalization due to unstable angina. Anti-oxLDL Abs (IgG class) were assayed at baseline, three and six weeks after ACS. The severity of coronary disease was evaluated by the Gensini score. We observed a decrease in anti-oxLDL Abs titers (p<0.002 vs. baseline), mainly in males (p=0.01), in those under 65 y (p=0.03), and in subjects with Gensini score above median (p=0.04). In conclusion, early decrease in circulating anti-oxLDL Abs is associated with coronary disease severity among subjects with MetS.
Life Sciences | 2015
Henrique Andrade Rodrigues da Fonseca; Francisco Antonio Helfenstein Fonseca; Lívia Campos do Amaral Silva Lins; Andrea Moreira Monteiro; Henrique Tria Bianco; Sergio A. Brandão; Rui Póvoa; Luiz Juliano; Antônio Martins Figueiredo-Neto; Paulo Boschcov; Magnus Gidlund; Maria Cristina de Oliveira Izar
AIMS The aim of this work was to evaluate the effects of treatment of hypertension on the autoantibodies to apolipoprotein B-derived peptides (anti-ApoB-D peptide Abs) response, inflammation markers and vascular function. MAIN METHODS Eighty-eight patients with hypertension (stage 1 or 2) were recruited and advised to receive perindopril (4mg), hydrochlorothiazide (25mg), or indapamide (1.5mg) for 12weeks in a blinded fashion. Office and 24-h ambulatory blood pressure monitoring (24h ABPM), flow-mediated dilatation (FMD), nitrate-induced dilatation (NID), titers of IgG and IgM anti-ApoB-D peptide Abs, hsCRP, and interleukins (IL-8 and IL-10) were evaluated at baseline and 12weeks after therapies. KEY FINDINGS All treatments reduced office BP, and improved FMD (P<0.05 vs. baseline). The NID was improved only in the perindopril arm (P<0.05 vs. baseline). The 24h-ABPM was reduced with perindopril and hydrochlorothiazide therapies (P<0.05 vs. baseline), but not with indapamide, and this effect was followed by increase in titers of IgM Anti-ApoB-D peptide Abs (P<0.05 vs. baseline), without modifications in titers IgG Anti-ApoB-D peptide Abs and interleukins. Multivariable regression analysis has shown that change in the titers of IgM anti-ApoB-D peptide was associated with the changes in FMD (β -0.347; P<0.05). SIGNIFICANCE These findings shed light to a possible modulator effect of the antihypertensive therapy on the natural immunity responses and vascular function.
Arquivos Brasileiros De Cardiologia | 2018
Maria Cristina de Oliveira Izar; Henrique Andrade Rodrigues da Fonseca; Carolina Nunes França; Valéria A. Machado; Carlos Ferreira; Francisco Antonio Helfenstein Fonseca
DOI: 10.5935/abc.20180191 Adiposis dolorosa, or Dercum’s disease, is a subcutaneous accumulation of fat in the body accompanied by intense, chronic, and symmetrical pain, often disabling, and usually not responsive to conventional analgesics. It was first described by Dercum, recognized as a separate disease in 1892,1 and further reported by White in 1899.2 Termed in the literature Dercum’s disease, Morbus Dercum, lipomatosis dolorosa, adiposalgia, adiposis dolorosa, and adipose tissue rheumatism, this condition is more prevalent in young women, aged 35 to 50 years, and affects preferably those in the post-menopause phase.1-3 Adiposis dolorosa can also occur in multiple familial lipomatosis, a condition associated with multiple lipomas.4 Other symptoms and signs include psychiatric (depression, anxiety, sleep disturbances, memory and concentration impairment), cardiovascular (tachycardia), pulmonary (shortness of breath), rheumatological (fatigue, weakness, joint and muscle aches) and gastrointestinal (bloating, constipation) disorders.3
PLOS ONE | 2016
Célia Regina de Oliveira Bittencourt; Maria Cristina de Oliveira Izar; Valdir Lauro Schwerz; Rui Manuel dos Santos Póvoa; Henrique Andrade Rodrigues da Fonseca; Marília Izar Helfenstein Fonseca; Henrique Tria Bianco; Carolina Nunes França; Carlos Eduardo dos Santos Ferreira; Francisco Antonio Helfenstein Fonseca
To evaluate the effects of long-term exposure to high-intensity training among professional runners on cardiac hypertrophy and subclinical atherosclerosis. Prospective study included runners of both sexes (n = 52) and age and gender matched controls (n = 57), without classical cardiovascular risk factors. Ventricular hypertrophy was quantified by echocardiography by linear method and carotid intima-media thickness (cIMT) by 2-D images obtained by ultrasonography. Endothelial function was evaluated by flow-mediated dilation (FMD). Steroid hormones were quantified by HPLC followed by LC-MS/MS. Higher left ventricular (LV) mass index was found in male athletes (p<0.0001 vs. other groups). When adjusted for gender, the degree of left ventricular mass index classified as mildly, moderately or severely abnormal was obtained in 26%, 35%, and 30%, respectively, of female athletes, and in 39%, 14%, and 21%, respectively, of male athletes. Higher ratio of the early (E) to late (A) ventricular filling velocities was found in athletes of both genders. Male athletes presented lower cIMT in the right (p = 0.012 vs. male controls) and left (p<0.0001 vs. male controls) common carotid arteries, without differences in cIMT between female athletes and controls. FMD results were similar among groups. Higher serum testosterone levels were found in male athletes (p<0.0001 vs. other groups) and they were correlated with LV mass (r = 0.50, p<0.0001). The chronic exposure of high-intensity training among professional runners of both genders was associated with increased ventricular mass and adaptive remodeling. Less subclinical atherosclerosis was found in male athletes. Differences in steroid hormones may account in part for these findings.
Arquivos Brasileiros De Cardiologia | 2014
Henrique Tria Bianco; Maria Cristina de Oliveira Izar; Henrique Andrade Rodrigues da Fonseca; Rui Manuel dos Santos Póvoa; José Francisco Kerr Saraiva; Adriana Costa e Forti; Paulo César Brandão Veiga Jardim; Luis Introcaso; Juan Carlos Yugar-Toledo; Xavier Ht; André Arpad Faludi; Francisco Antonio Helfenstein Fonseca
Background Patients with diabetes are in extract higher risk for fatal cardiovascular events. Objective To evaluate major predictors of mortality in subjects with type 2 diabetes. Methods A cohort of 323 individuals with type 2 diabetes from several regions of Brazil was followed for a long period. Baseline electrocardiograms, clinical and laboratory data obtained were used to determine hazard ratios (HR) and confidence interval (CI) related to cardiovascular and total mortality. Results After 9.2 years of follow-up (median), 33 subjects died (17 from cardiovascular causes). Cardiovascular mortality was associated with male gender; smoking; prior myocardial infarction; long QTc interval; left ventricular hypertrophy; and eGFR <60 mL/min. These factors, in addition to obesity, were predictors of total mortality. Cardiovascular mortality was adjusted for age and gender, but remained associated with: smoking (HR = 3.8; 95% CI 1.3-11.8; p = 0.019); prior myocardial infarction (HR = 8.5; 95% CI 1.8-39.9; p = 0.007); eGFR < 60 mL/min (HR = 9.5; 95% CI 2.7-33.7; p = 0.001); long QTc interval (HR = 5.1; 95% CI 1.7-15.2; p = 0.004); and left ventricular hypertrophy (HR = 3.5; 95% CI 1.3-9.7; p = 0.002). Total mortality was associated with obesity (HR = 2.3; 95% CI 1.1-5.1; p = 0.030); smoking (HR = 2.5; 95% CI 1.0-6.1; p = 0.046); prior myocardial infarction (HR = 3.1; 95% CI 1.4-6.1; p = 0.005), and long QTc interval (HR = 3.1; 95% CI 1.4-6.1; p = 0.017). Conclusions Biomarkers of simple measurement, particularly those related to target-organ lesions, were predictors of mortality in subjects with type 2 diabetes.
Cell Biochemistry and Biophysics | 2013
Henrique Andrade Rodrigues da Fonseca; Francisco Antonio Helfenstein Fonseca; Andrea Moreira Monteiro; Henrique Tria Bianco; Paulo Boschcov; Sergio A. Brandão; Luiz Juliano; Magnus Gidlund; Maria Cristina de Oliveira Izar
International Journal of Cardiology | 2012
Henrique Andrade Rodrigues da Fonseca; Francisco Antonio Helfenstein Fonseca; Andrea Moreira Monteiro; Nelson Carvalho Farias; Henrique Tria Bianco; Sergio A. Brandão; Rui Póvoa; Magnus Gidlund; Maria Cristina de Oliveira Izar
Acta Scientiarum. Health Science | 2010
Henrique Andrade Rodrigues da Fonseca; Rodolfo André Dellagrana; Luiz Rodrigo Augustemak de Lima; Edson Itaru Kaminagakura
Cell Biochemistry and Biophysics | 2016
Henrique Andrade Rodrigues da Fonseca; Célia Regina de Oliveira Bittencourt; Francisco Antonio Helfenstein Fonseca; Andrea Moreira Monteiro; Priscila Robertina dos Santos; L.M. Camargo; Luiz A. R. Costa; Alexandre Murad; Magnus Gidlund; Antônio Martins Figueiredo-Neto; Maria Cristina de Oliveira Izar
International Journal of Cardiology | 2015
Valéria A. Machado; Francisco Antonio Helfenstein Fonseca; Henrique Andrade Rodrigues da Fonseca; Daniela T. Malina; Waléria T. Fonzar; Sílvio A. Barbosa; José Marcos Santana; Maria Cristina de Oliveira Izar
Collaboration
Dive into the Henrique Andrade Rodrigues da Fonseca's collaboration.
Francisco Antonio Helfenstein Fonseca
Icahn School of Medicine at Mount Sinai
View shared research outputsMaria Cristina de Oliveira Izar
Icahn School of Medicine at Mount Sinai
View shared research outputsFrancisco Antonio Helfenstein Fonseca
Icahn School of Medicine at Mount Sinai
View shared research outputsMaria Cristina de Oliveira Izar
Icahn School of Medicine at Mount Sinai
View shared research outputs